C9orf72 gene located on chromosome 9p21.2, encoding protein in brain regions. Disease-causing mutations discovered in 2011 by Mayo Clinic and NIH teams. Most common mutation associated with familial FTD/ALS in Caucasians
RAK Hospital provides tertiary care services in Northern Emirates. Super Specialist doctors deliver care through collaborative model. Hospital focuses on patient-centered care and personalized attention
Cancer symptoms vary widely and can be non-specific. Skin changes, unusual lumps, and unhealing sores may indicate cancer. Unexplained weight loss over 10 pounds suggests pancreatic or stomach cancer. Early symptoms can resemble common cold symptoms
DMD is a rapidly progressive muscular dystrophy affecting 1 in 3500 male births worldwide. Caused by mutation in DMD gene, inherited in X-linked recessive pattern. Males inherit condition from affected parent, females are carriers. About 20% of carrier females show symptoms
New guidelines cover various cardiomyopathy subtypes and clinical phases. Multidisciplinary approach and family involvement emphasized. Genetic testing and multimodality imaging recommended for diagnosis
Cavernoma is a cluster of abnormal blood vessels in brain and spinal cord. Appears as raspberry-shaped, filled with slow-flowing blood. Can vary in size from millimetres to several centimetres